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Un-I-Med, Inc.

FDA Regulatory Profile

Un-I-Med, Inc. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
May 3, 1995

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances2Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Unimed
Same company group		0010—

Recent 510(k) Clearances

K-NumberDeviceDate
K945191ENDOSCOPIC ACCESSORYMay 3, 1995
K903480HANN-VAC TM, DISPOSABLE,SUCTION CATHETEROct 1, 1991

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.